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Hydrogen Peroxide → 4-Bromo-1H-indole-6-carboxamide
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Hydrogen Peroxide | HCID 784 | — |
| 反応物 | Water | HCID 962 | — |
| 反応物 | Sodium Hydroxide | HCID 14798 | — |
| 反応物 | 4-bromo-1H-indole-6-carbonitrile | HCID 24728883 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 生成物 | 4-Bromo-1H-indole-6-carboxamide | HCID 66870555 | 97.6% |
反応手順
A solution of 4-bromo-1H-indole-6-carbonitrile (1 g, 4.50 mmol) in methanol (10 mL) was treated with 30% aqueous hydrogen peroxide (2.7 mL, 4.95 mmol) and a 1 M aqueous sodium hydroxide solution (5 mL) then heated at 40° C. for 1 h. The reaction mixture was cooled, treated with water and cooled in an ice-bath. The resulting precipitate was collected by filtration, washed with water and dried in vacuo to obtain 4-bromo-1H-indole-6-carboxylic acid amide (1.05 g, 97%), which was transformed into the title boronic ester by the general method (Scheme 1) (0.80 g, 67%).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08697693B2 |
| 出典データセット | uspto-grants-2014_04 |
| ORD ID | ord-5c2e0d2757b24f4fb0c9ce4d181c28b8 |
| 出典メモ | uspto-grants-2014_04 |